Publication Type Academic Article
Authors Swerdlow R, de Leon M, Marcus D
Journal J Alzheimers Dis Rep
Volume 5
Issue 1
Pagination 135-141
Date Published 02/24/2021
ISSN 2542-4823
Abstract BACKGROUND: Alzheimer's disease (AD) features perturbed brain glucose utilization, which could contribute to brain bioenergetic failure. This led some to consider using ketone bodies to enhance AD brain bioenergetics and treat AD. OBJECTIVE: We evaluated the rate at which brain homogenates from persons with Alzheimer's disease (AD) metabolize D-β-hydroxybutyrate (BHB). METHODS: We homogenized pieces of temporal cortex from frozen autopsy brains obtained from recently deceased AD subjects (n = 4), and age-matched subjects that did not have clinical AD (n = 3). Measuring the rate of CO2 production that followed the introduction of radiolabeled BHB to the homogenates yielded a BHB utilization rate. RESULTS: Compared to the control homogenates, the BHB-supported CO2 production rate was 66%lower in the AD homogenates (p < 0.05). CONCLUSIONS: AD brains can utilize BHB, albeit less robustly than control brains. In conjunction with a previous study that demonstrated reduced glucose utilization in AD brain homogenates, our BHB data provide further evidence of AD brain mitochondrial dysfunction or altered mitochondrial biology.
DOI 10.3233/ADR-210002
PubMed ID 33782666
PubMed Central ID PMC7990458
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